FDA UDI In Commercial Distribution 🇺🇸 United States

Duette™

DI: 10852732004033 · Model: D-10014 · POIESIS MEDICAL, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
Duette™
Primary DI
10852732004033
Version / Model
D-10014
Company Name
POIESIS MEDICAL, LLC
Labeler DUNS
831415109
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2017-01-27
Public Version
9
Public Version Date
2020-12-04
Public Version Status
Update
Public Device Record Key
4bd95a2b-4f17-452c-bc26-160c52e74e9b

Device Description

14FR Duette™ Indwelling Urinary Catheter

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
MR Safe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
EZL CATHETER, RETENTION TYPE, BALLOON

GMDN Terms

Code Name
34917 Indwelling urethral drainage balloon catheter, non-antimicrobial

Identifiers

Type ID
Primary 10852732004033
Unit of Use 00852732004029

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K941488 000

Device Sizes

Type Value Unit Text
Catheter Gauge 14 French

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-10 – 50 Degrees Celsius
Type
Special Storage Condition, Specify
Special Conditions
Keep Out of Sunlight